1. Distinct Stem Cell Populations Regenerate the Follicle and Interfollicular Epidermis 
Vered Levy, Catherine Lindon, Brian D. Harfe, Bruce A. Morgan 
Developmental Cell 
Volume 9, Issue 6, Pages (December 2005)
DOI: /j.devcel
Copyright © 2005 Elsevier Inc. Terms and Conditions

2. Figure 1 Structure of the Hair Follicle
The structure of the pilosebaceous unit, comprised of the hair follicle and sebaceous gland, is shown during the anagen (left) and telogen (right) phases of the hair cycle with structures referred to in the text labeled. Note that the niche of the follicular stem cells is a restricted region of the permanent portion of the hair follicle (structures above the black, dotted line) adjacent to the attachment site of the arrector pili muscle. Because this is difficult to identify unambiguously, we use the broader definition of the follicular epithelium of the telogen follicle between the mouth of the sebaceous gland and the secondary germ that encompasses the niche of the stem cells of the bulge. Structures below the red, dotted line comprise the “definitive follicle” defined empirically in this work. The sebaceous gland and infundibulum lie outside the “definitive follicle.”
Developmental Cell 2005 9, DOI: ( /j.devcel )
Copyright © 2005 Elsevier Inc. Terms and Conditions

3. Figure 2
Shh Expression in Embryonic Skin Allows for Lineage Analysis of the Follicle with ShhGFPcre
(A and B) In situ hybridization reveals the expression of Shh (purple) during follicle development. The border between epithelium and dermis is marked by a dotted, red line. (A) At stage 1 (hair germ), the follicular placode cells express Shh. (B) At stage 3 (hair peg), Shh expression is localized to the cells at the base of the hair peg in contact with the dermal papilla.
(C) GFP fluorescence reveals the expression of the GFPcre fusion protein in the epidermal placodes of skin from a ShhGFPcre embryo.
(D and E) Detection of β-galactosidase activity (blue) in skin from a ShhGFPcre embryo. (D) Although Shh expression is restricted to cells at the base of the hair peg at this stage (see [B]), all cells of the hair peg are stained blue to reveal that the cells of the upper follicle are derived from cells that once expressed Shh. The interplacodal epidermis is not labeled. Immunohistochemical detection of keratin 14 (brown) identifies the basal epidermis and follicular epithelium. (E) Whole-mount view of an E15.5 embryo reveals labeling of both primary and incipient secondary follicles (faint dots in inset), while interfollicular skin is unlabeled.
Developmental Cell 2005 9, DOI: ( /j.devcel )
Copyright © 2005 Elsevier Inc. Terms and Conditions

4. Figure 3
The Epithelium of the Mature Hair Follicle Is Derived from Cells that Expressed Shh
(A–C) At p18, hair follicles in ShhGFPcre;R26R skin have entered the resting phase at the end of the first hair cycle. (A) Whole-mount and (B and C) section views reveal that the follicles are labeled (blue), while interfollicular skin is not. Immunohistochemical detection of keratin 14 (brown) identified the basal layer of the epidermis and outer root sheath of the hair follicle. (B) The only blue cells in the epidermis (asterisk) are in the suprabasal layers and are associated with the mouth of a follicle in another plane observed below in glancing section (arrowhead). (C) A higher-magnification view demonstrates that the entire region below the mouth of the sebaceous gland, including any more restrictive definition of the follicular bulge (bracket), is labeled. An arrowhead indicates unlabeled cells in the upper follicle.
(D) In the absence of cre, R26R skin remains unlabeled.
(E) Detection of β-galactosidase in K14cre;R26R skin, in which cre is expressed throughout the basal layer and ORS, confirms the ability to detect the expression of this reporter in interfollicular epidermis.
Developmental Cell 2005 9, DOI: ( /j.devcel )
Copyright © 2005 Elsevier Inc. Terms and Conditions

5. Figure 4
The Stem Cells of the Follicular Bulge Do Not Normally Contribute to the Interfollicular Epidermis
(A–E) β-galactosidase activity (blue) in ShhGFPcre;R26R skin from mice at (A) 6 months and (B–E) 18 months of age. (A) At 6 months, several hair cycles have occurred. The follicles remain labeled, confirming the effective labeling of follicular stem cells. The epidermis, counterstained with keratin 1 to identify the suprabasal layer, is unlabeled. No blue cells are observed in the basal layer, immediately beneath the layer stained with K1. Note that the interfollicular epidermis has expanded considerably with age (compare to Figure 3B) without the contribution of cells from the follicular bulge. (B) The epidermis remains unlabeled, while the follicles are blue in mice near the end of a normal lifespan. (C) Sections costained with K14 confirm that the follicles remain labeled, while the epidermis is unlabeled. While the definitive follicle below the sebaceous gland is consistently labeled, the infundibulum of some follicles is only partially labeled (arrowhead). The bulge region (bracket) and arrector pili muscle (arrow) of this telogen-stage follicle are indicated. (D) More lightly stained samples confirm complete labeling of the definitive follicle. In this sample, the infundibulum and the sebaceous gland are partially labeled. (E) Whole-mount view of ShhGFPcre;R26R skin harvested at 18 months.
(F and G) High- and low-magnification views of sections from k14cre; R26R skin counterstained with keratin 14 (brown) confirm the ability to detect β-galactosidase activity (blue) in all keratinocytes of the skin.
Developmental Cell 2005 9, DOI: ( /j.devcel )
Copyright © 2005 Elsevier Inc. Terms and Conditions